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Long-term outcome of defibrillator recipients included in the federal audit conducted by the department of justice

机译:除颤器接受者的长期结果已纳入司法部进行的联邦审计中

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Institutions across the United States have been subjected to a federal audit for defibrillator implantable cardioverter defibrillator [ICD] implantations that violated the Centers for Medicare and Medicaid payment policy. We examined the long-term outcome of ICD recipients whose implantation procedures were audited by the Department of Justice (DOJ). Patients (n = 225) included in the DOJ audit at the University of Pittsburgh Medical Center between the years 2003 and 2010 were followed to the end point of all-cause mortality. A cohort of 206 consecutive and contemporary ICD recipients not included in the federal audit served as controls. Compared with the controls, the audited cases were older (p <0.001), had more preserved ejection fraction (p <0.001), and were less likely to be implanted for a primary prevention indication (p = 0.001). They also had significantly shorter time from myocardial infarction (p <0.001) or revascularization (p <0.001) to ICD implantation. Over a median follow-up of 3.6 years, 187 patients died and 71 received ICD therapy for ventricular arrhythmias. Patients whose cases were audited had worse survival compared with controls (hazard ratio 1.41, 95% confidence interval 1.05 to 1.90, p = 0.023) even after correcting for differences in baseline characteristics (hazard ratio 1.46, 95% confidence interval 1.05 to 2.02, p = 0.023). Rates of appropriate and inappropriate ICD therapies were similar between the audited cases and controls. In conclusion, patients whose ICD implantations were audited by the DOJ have worse long-term survival compared with nonaudited control patients. These data support compliance with the Centers for Medicare and Medicaid guidelines when the individual patient's clinical condition allows it.
机译:美国各地的机构都接受了联邦医疗机构对植入除纤颤器的可植入式心脏复律除颤器[ICD]的审查,这违反了医疗保险和医疗补助中心的付款政策。我们检查了ICD接受者的长期结果,其植入程序已由司法部(DOJ)审核。匹兹堡大学医学中心在2003年至2010年之间纳入DOJ审核的患者(n = 225)被追踪到全因死亡率的终点。 206名连续的和同时代的ICD接受者(未包括在联邦审计中)作为对照。与对照组相比,经审核的病例年龄更大(p <0.001),射血分数得以保留(p <0.001),并且为一级预防适应症而植入的可能性较小(p = 0.001)。从心肌梗塞(p <0.001)或血运重建(p <0.001)到ICD植入,他们的时间也明显缩短。在3.6年的中位随访中,有187例患者死亡,71例接受了ICD治疗室性心律失常。即使校正基线特征的差异(风险比1.46,95%置信区间1.05至2.02,p),接受检查的患者与对照组相比,生存率较对照组(危险比1.41,95%置信区间1.05至1.90,p = 0.023)差。 = 0.023)。适当的和不适当的ICD疗法的比率在被审计的病例和对照之间是相似的。总之,与未经审核的对照患者相比,经美国司法部审核过ICD植入的患者的长期生存期较差。当个别患者的临床状况允许时,这些数据支持符合医疗保险中心和医疗补助准则的要求。

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